"Deutschland" automatic plasma platen system - Taiwan Registration 58171ba3eb2b044207151f938d83a7bb
Access comprehensive regulatory information for "Deutschland" automatic plasma platen system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 58171ba3eb2b044207151f938d83a7bb and manufactured by FRESENIUS KABI AG;; SANMINA-SCI. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FRESENIUS KABI AG, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Registration Details
58171ba3eb2b044207151f938d83a7bb
DHA00602181802
Product Details
For details, it is Chinese approved copy of the imitation order
B Hematology, pathology, and genetics
B.0002 Blood Component Extraction Apparatus
Input;; Contract manufacturing
Dates and Status
Nov 30, 2010
Mar 28, 2016
Aug 14, 2018
Cancellation Information
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